Variant · Snv
PTPN13 NM_080683.3(PTPN13):c.6614G>A (p.Arg2205Gln)
CI-VAR-00179557Explore in graph →p.Arg2205GlnNM_080683.3:c.6614G>AClinVar 1049428 rs61750816
Curated evidence
Evidence by cancer (0 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 1049428 | Likely benign | criteria provided, single submitter | 1 | Sarcoma; Thymoma; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Melanoma; Hepatocellular carcinoma; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Uterine carcinosarcoma; Thyroid cancer, nonmedullary, 1; Cervical cancer | germline | 3 | — | clinvar |